• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Flexibility and constraint in the nucleosome core landscape of Caenorhabditis elegans chromatin.秀丽隐杆线虫染色质核小体核心景观中的灵活性与限制
Genome Res. 2006 Dec;16(12):1505-16. doi: 10.1101/gr.5560806. Epub 2006 Oct 12.
2
A high-resolution, nucleosome position map of C. elegans reveals a lack of universal sequence-dictated positioning.秀丽隐杆线虫的高分辨率核小体定位图谱显示缺乏通用的序列决定定位。
Genome Res. 2008 Jul;18(7):1051-63. doi: 10.1101/gr.076463.108. Epub 2008 May 13.
3
Chromatin structure of the yeast URA3 gene at high resolution provides insight into structure and positioning of nucleosomes in the chromosomal context.酵母URA3基因的高分辨率染色质结构为深入了解染色体环境中核小体的结构和定位提供了线索。
J Mol Biol. 1996 Apr 19;257(5):919-34. doi: 10.1006/jmbi.1996.0212.
4
Nucleosome fragility is associated with future transcriptional response to developmental cues and stress in C. elegans.核小体的脆弱性与秀丽隐杆线虫未来对发育信号和应激的转录反应相关。
Genome Res. 2017 Jan;27(1):75-86. doi: 10.1101/gr.208173.116. Epub 2016 Nov 14.
5
Single-base resolution nucleosome mapping on DNA sequences.单碱基分辨率核小体在 DNA 序列上的作图。
J Biomol Struct Dyn. 2010 Aug;28(1):107-22. doi: 10.1080/07391102.2010.10507347.
6
Painting a perspective on the landscape of nucleosome positioning.描绘核小体定位景观的透视。
J Biomol Struct Dyn. 2010 Jun;27(6):795-802. doi: 10.1080/073911010010524946.
7
Three sequence rules for chromatin.染色质的三条序列规则。
J Biomol Struct Dyn. 2006 Apr;23(5):559-66. doi: 10.1080/07391102.2006.10507081.
8
Visible periodicity of strong nucleosome DNA sequences.强核小体DNA序列的可见周期性。
J Biomol Struct Dyn. 2015;33(1):1-9. doi: 10.1080/07391102.2013.855143. Epub 2013 Nov 22.
9
Global remodeling of nucleosome positions in C. elegans.线虫中核小体位置的全局重塑。
BMC Genomics. 2013 Apr 26;14:284. doi: 10.1186/1471-2164-14-284.
10
Combined micrococcal nuclease and exonuclease III digestion reveals precise positions of the nucleosome core/linker junctions: implications for high-resolution nucleosome mapping.联合使用微球菌核酸酶和核酸外切酶 III 消化可揭示核小体核心/连接区的精确位置:对高分辨率核小体作图的启示。
J Mol Biol. 2013 Jun 12;425(11):1946-1960. doi: 10.1016/j.jmb.2013.02.026. Epub 2013 Feb 28.

引用本文的文献

1
Interrogating the regulatory epigenome of cellular senescence.探究细胞衰老的调控表观基因组。
Cell Mol Life Sci. 2025 Aug 31;82(1):328. doi: 10.1007/s00018-025-05848-w.
2
SMAdd-seq: probing chromatin accessibility with small molecule DNA intercalation and nanopore sequencing.SMAdd-seq:利用小分子DNA嵌入和纳米孔测序探测染色质可及性
Nucleic Acids Res. 2025 Jul 19;53(14). doi: 10.1093/nar/gkaf671.
3
CGC1, a new reference genome for .CGC1,一个用于……的新参考基因组。 (原文不完整,翻译只能到这里)
Genome Res. 2025 Aug 1;35(8):1902-1918. doi: 10.1101/gr.280274.124.
4
CGC1, a new reference genome for .CGC1,一种用于……的新参考基因组。 (原文不完整,翻译可能不太准确,需结合完整内容进一步完善)
bioRxiv. 2024 Dec 6:2024.12.04.626850. doi: 10.1101/2024.12.04.626850.
5
High-throughput capture of transcription factor-driven epigenome dynamics using PHILO ChIP-seq.使用PHILO ChIP-seq高通量捕获转录因子驱动的表观基因组动态变化。
Nucleic Acids Res. 2024 Dec 11;52(22):e105. doi: 10.1093/nar/gkae1123.
6
KSHV genome harbors both constitutive and lytically induced enhancers.卡波西肉瘤相关疱疹病毒基因组包含组成型和裂解诱导型增强子。
J Virol. 2024 Jun 13;98(6):e0017924. doi: 10.1128/jvi.00179-24. Epub 2024 May 2.
7
Probing chromatin accessibility with small molecule DNA intercalation and nanopore sequencing.利用小分子DNA嵌入和纳米孔测序探测染色质可及性
bioRxiv. 2024 Mar 22:2024.03.20.585815. doi: 10.1101/2024.03.20.585815.
8
Canalizing cell fate by transcriptional repression.通过转录抑制来调控细胞命运。
Mol Syst Biol. 2024 Mar;20(3):144-161. doi: 10.1038/s44320-024-00014-z. Epub 2024 Feb 1.
9
Multimodal epigenetic sequencing analysis (MESA) of cell-free DNA for non-invasive colorectal cancer detection.基于游离细胞 DNA 的多模态表观遗传学测序分析(MESA)用于非侵入性结直肠癌检测。
Genome Med. 2024 Jan 16;16(1):9. doi: 10.1186/s13073-023-01280-6.
10
DeepCAC: a deep learning approach on DNA transcription factors classification based on multi-head self-attention and concatenate convolutional neural network.DeepCAC:一种基于多头自注意力和串联卷积神经网络的 DNA 转录因子分类深度学习方法。
BMC Bioinformatics. 2023 Sep 18;24(1):345. doi: 10.1186/s12859-023-05469-9.

本文引用的文献

1
DNA motifs and sequence periodicities.DNA基序与序列周期性
In Silico Biol. 2006;6(1-2):71-8.
2
Structural analysis of hyperperiodic DNA from Caenorhabditis elegans.秀丽隐杆线虫超周期DNA的结构分析。
Nucleic Acids Res. 2006 May 31;34(10):3057-66. doi: 10.1093/nar/gkl397. Print 2006.
3
Unusual DNA structures associated with germline genetic activity in Caenorhabditis elegans.与秀丽隐杆线虫种系遗传活性相关的异常DNA结构。
Genetics. 2006 Jul;173(3):1259-73. doi: 10.1534/genetics.106.057364. Epub 2006 Apr 28.
4
Toward a physical map of the genome of the nematode Caenorhabditis elegans.构建秀丽隐杆线虫基因组物理图谱。
Proc Natl Acad Sci U S A. 1986 Oct;83(20):7821-5. doi: 10.1073/pnas.83.20.7821.
5
Three sequence rules for chromatin.染色质的三条序列规则。
J Biomol Struct Dyn. 2006 Apr;23(5):559-66. doi: 10.1080/07391102.2006.10507081.
6
Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS).使用大规模平行签名测序(MPSS)对DNA酶超敏位点进行全基因组图谱绘制。
Genome Res. 2006 Jan;16(1):123-31. doi: 10.1101/gr.4074106. Epub 2005 Dec 12.
7
Analysis of homologous gene clusters in Caenorhabditis elegans reveals striking regional cluster domains.对秀丽隐杆线虫中同源基因簇的分析揭示了显著的区域簇结构域。
Genetics. 2006 Jan;172(1):127-43. doi: 10.1534/genetics.104.040030. Epub 2005 Nov 15.
8
Genome sequencing in microfabricated high-density picolitre reactors.微制造高密度皮升反应器中的基因组测序
Nature. 2005 Sep 15;437(7057):376-80. doi: 10.1038/nature03959. Epub 2005 Jul 31.
9
Genome-scale identification of nucleosome positions in S. cerevisiae.酿酒酵母中核小体位置的全基因组规模鉴定。
Science. 2005 Jul 22;309(5734):626-30. doi: 10.1126/science.1112178. Epub 2005 Jun 16.
10
Intrinsic histone-DNA interactions and low nucleosome density are important for preferential accessibility of promoter regions in yeast.内在的组蛋白与DNA相互作用以及低核小体密度对于酵母中启动子区域的优先可及性很重要。
Mol Cell. 2005 Jun 10;18(6):735-48. doi: 10.1016/j.molcel.2005.05.003.

秀丽隐杆线虫染色质核小体核心景观中的灵活性与限制

Flexibility and constraint in the nucleosome core landscape of Caenorhabditis elegans chromatin.

作者信息

Johnson Steven M, Tan Frederick J, McCullough Heather L, Riordan Daniel P, Fire Andrew Z

机构信息

Department of Pathology, Stanford University School of Medicine, Stanford, California 94305-5324, USA.

出版信息

Genome Res. 2006 Dec;16(12):1505-16. doi: 10.1101/gr.5560806. Epub 2006 Oct 12.

DOI:10.1101/gr.5560806
PMID:17038564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1665634/
Abstract

Nucleosome positions within the chromatin landscape are known to serve as a major determinant of DNA accessibility to transcription factors and other interacting components. To delineate nucleosomal patterns in a model genetic organism, Caenorhabditis elegans, we have carried out a genome-wide analysis in which DNA fragments corresponding to nucleosome cores were liberated using an enzyme (micrococcal nuclease) with a strong preference for cleavage in non-nucleosomal regions. Sequence analysis of 284,091 putative nucleosome cores obtained in this manner from a mixed-stage population of C. elegans reveals a combined picture of flexibility and constraint in nucleosome positioning. As has previously been observed in studies of individual loci in diverse biological systems, we observe areas in the genome where nucleosomes can adopt a wide variety of positions in a given region, areas with little or no nucleosome coverage, and areas where nucleosomes reproducibly adopt a specific positional pattern. In addition to illuminating numerous aspects of chromatin structure for C. elegans, this analysis provides a reference from which to begin an investigation of relationships between the nucleosomal pattern, chromosomal architecture, and lineage-based gene activity on a genome-wide scale.

摘要

染色质景观中的核小体位置是DNA对转录因子和其他相互作用成分可及性的主要决定因素。为了描绘模式遗传生物秀丽隐杆线虫中的核小体模式,我们进行了全基因组分析,其中使用一种对非核小体区域的切割有强烈偏好的酶(微球菌核酸酶)释放与核小体核心相对应的DNA片段。以这种方式从秀丽隐杆线虫的混合发育阶段群体中获得的284,091个推定核小体核心的序列分析揭示了核小体定位中灵活性和限制性的综合情况。正如先前在不同生物系统中对单个基因座的研究所观察到的那样,我们在基因组中观察到这样一些区域:在给定区域内核小体可以采用多种位置;几乎没有或没有核小体覆盖的区域;以及核小体可重复采用特定位置模式的区域。除了阐明秀丽隐杆线虫染色质结构的众多方面之外,该分析还提供了一个参考,以便在全基因组范围内开始研究核小体模式、染色体结构和基于谱系的基因活性之间的关系。